Jasmine Davis, M.S.
About Jasmine Davis, M.S.
Jasmine Davis, M.S., is the Senior Manager of Quality Operations ExM NA at Bristol Myers Squibb and the owner of Hire Up Career Service. She has extensive experience in quality assurance and regulatory affairs within the pharmaceutical industry.
Current Position at Bristol Myers Squibb
Jasmine Davis, M.S. holds the position of Senior Manager Quality Operations ExM NA at Bristol Myers Squibb. Based in New Jersey, United States, she oversees quality operations in external manufacturing. Her role involves managing quality standards and ensuring compliance with regulatory requirements, especially focusing on solid oral dose and sterile manufacturing environments.
Owner of Hire Up Career Service
In addition to her position at Bristol Myers Squibb, Jasmine Davis is the owner of Hire Up Career Service. Her entrepreneurial venture focuses on career services, showcasing her skills in business management and her commitment to helping others advance their careers. This dual role highlights her capabilities in both the corporate and entrepreneurial spheres.
Previous Roles in Quality Assurance
Jasmine Davis has a robust background in quality assurance within the pharmaceutical industry. She previously worked as Quality Assurance Manager at Amring Pharmaceuticals Inc. from 2019 to 2022. Prior to that, she served in various senior roles at Takeda, including Senior Quality Assurance Specialist II and I, spanning from 2016 to 2019. Her extensive experience also includes positions at Endo Pharmaceuticals, Shire Pharmaceuticals, Nuron Biotech Inc., and WuXi AppTec.
Educational Background
Jasmine Davis earned her Master of Science (M.S.) in Quality Assurance/Regulatory Affairs from Temple University Graduate School, studying from 2014 to 2017. She also holds a Bachelor of Science (B.S.) in Biology from Morgan State University, where she studied from 2001 to 2005. Her academic background provides a strong foundation for her extensive career in quality assurance and regulatory affairs.
Experience in Biotechnology and Regulatory Affairs
Jasmine Davis is well-versed in biotechnology, regulatory requirements, SAP ERP, and software documentation. Her extensive experience in overseeing external manufacturing across all GXP environments demonstrates her adept handling of quality assurance processes and regulatory affairs. She has a demonstrated history of ensuring compliance and maintaining quality standards in the pharmaceutical industry.